Canonical Allele Identifier: CA2269946982

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63490953G= , CM000679.2:g.63490953G=	GRCh38
NC_000017.10:g.61568314G= , CM000679.1:g.61568314G=	GRCh37
NC_000017.9:g.58922046G=	NCBI36
NG_011648.1:g.18881G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000789.4:c.2642-1G= MANE Select	NP_000780.1:n.2642-1G=
ENST00000290866.10:c.2642-1G= MANE Select	ENSP00000290866.4:n.2642-1G=
NM_000789.3:c.2642-1G=	NP_000780.1:n.2642-1G=
NM_001178057.1:c.920-1G=	NP_001171528.1:n.920-1G=
NM_001178057.2:c.920-1G=	NP_001171528.1:n.920-1G=
NM_001382700.1:c.2075-1G=	NP_001369629.1:n.2075-1G=
NM_001382701.1:c.1790-1G=	NP_001369630.1:n.1790-1G=
NM_001382702.1:c.380-1G=	NP_001369631.1:n.380-1G=
NM_152830.2:c.920-1G=	NP_690043.1:n.920-1G=
NM_152830.3:c.920-1G=	NP_690043.1:n.920-1G=
NR_168483.1:n.1020-1G=
ENST00000290863.10:c.920-1G=	ENSP00000290863.6:n.920-1G=
ENST00000290866.9:c.2642-1G=	ENSP00000290866.4:n.2642-1G=
ENST00000413513.7:c.920-1G=	ENSP00000392247.3:n.920-1G=
ENST00000428043.5:c.2642-1G=	ENSP00000397593.2:n.2642-1G=
ENST00000577418.5:n.146+925G=
ENST00000577647.2:c.920-1G=	ENSP00000464149.1:n.920-1G=
ENST00000578839.5:c.*520-1G=	ENSP00000462110.2:n.*520-1G=
ENST00000579314.5:c.*371-1G=	ENSP00000462599.1:n.*371-1G=
ENST00000582761.1:c.410-1G=	ENSP00000462909.1:n.410-1G=
ENST00000583645.1:n.606G=
ENST00000584865.5:n.588-1G=
XM_005257110.1:c.2093-1G=	XP_005257167.1:n.2093-1G=
XM_006721737.2:c.980-1G=	XP_006721800.2:n.980-1G=
XM_006721737.3:c.980-1G=	XP_006721800.2:n.980-1G=